# K132658: Hemoclip Traditional Ligating Clips, Hemoclip Plus Ligating Clips, Horizon Ligting Clips

- Pathway: 510(k) (Traditional)
- Applicant: Teleflex Medical
- Decided: Nov 27, 2013 after 93 days
- Product code: FZP (Clip, Implantable)
- Device class: 2
- Regulation: 21 CFR 878.4300
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K841547 (1984). 2 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K982313: Horizon Titanium Clips, Horizon Tantalum Clips, Weck Closure Systems (1998) Summary page 2.
- K841547: Hemoclip Ligating Clips Med/SML, Edward Weck, Inc. (1984) Summary page 2.

## Most influential descendants
- K192711: Dannik Titanium Ligation Clip (2019), 0 descendants of its own

## Recalls of this device
- Apr 28, 2023 · Class II · Z-1663-2023: Teleflex LLC is initiating this voluntary field corrective action because the clip cartridges for the affected product is missing a key feature that restricts the application of the clip to the applie

## Indications for use
Weck® Ligating Clips are intended for use in procedures involving vessels or anatomic structures for which the surgeon determines ligating clips are the best choice. Surgeons should select the size, type and material of the clip based upon their experience, judgment and needs.

Source page: https://510kreport.com/device/K132658
Methodology: https://510kreport.com/methodology